
Nivolumab provides improved effectiveness and safety compared with docetaxel as a second‐line treatment for advanced non‐small cell lung cancer: A systematic review and meta‐analysis
Author(s) -
Xu Zheng,
Yi Fengming,
Yu Dongliang,
Xu Jianjun,
Wei Yiping,
Zhang Wenxiong
Publication year - 2019
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.1966
Subject(s) - nivolumab , docetaxel , medicine , oncology , lung cancer , nausea , adverse effect , rash , hazard ratio , chemotherapy , meta analysis , cancer , confidence interval , immunotherapy
Background As an inhibitor of programmed death‐1 (PD‐1) protein, nivolumab has been shown to be effective in various cancers. We thus conducted this meta‐analysis to compare the relative efficacy of nivolumab vs docetaxel‐based chemotherapy as a second‐line treatment for previously treated advanced non‐small cell lung cancer (NSCLC). Methods Relevant studies were identified through searches of databases and conference proceedings. Progression‐free survival (PFS), overall survival (OS), drug responses, and adverse effects (AEs) were assessed as the primary endpoints. Results After screening, we included six studies (949 patients) in the final analysis. Nivolumab showed better efficacy in terms of the PFS (hazard ratios [HR]: 0.70, P = 0.03), OS (HR: 0.70, P < 0.00001), objective response rate (ORR) (risk ratios [RR]: 1.73, P = 0.0008), total AEs (RR: 0.77, P = 0.006), and grade 3‐5 AEs (RR: 0.18, P < 0.00001) than docetaxel. The anti‐tumor efficacy of nivolumab for NSCLC in terms of both PFS and OS was positively correlated with the level of PD‐L1 expression. In the nivolumab treatment arm, the 10 most‐reported AEs were fatigue (15.7%), nausea (10.8%), decreased appetite (10.3%), asthenia (9.8%), diarrhea (7.5%), rash (7.5%), arthralgia (5.4%), vomiting (4.4%), constipation (3.5%), and pyrexia (3.3%). Conclusions For advanced NSCLC, nivolumab is a better therapy in terms of both anti‐tumor efficacy and safety than docetaxel‐based chemotherapy. More high‐quality randomized controlled trials are needed to confirm these results.